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rs1057518201

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518201(-;-)
Make rs1057518201(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2081637
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057518201
dbSNP (old)rs1057518201
ClinGenrs1057518201
ebirs1057518201
HLIrs1057518201
Exacrs1057518201
Gnomadrs1057518201
Varsomers1057518201
Maprs1057518201
PheGenIrs1057518201
Biobankrs1057518201
1000 genomesrs1057518201
hgdprs1057518201
ensemblrs1057518201
gopubmedrs1057518201
geneviewrs1057518201
scholarrs1057518201
googlers1057518201
pharmgkbrs1057518201
gwascentralrs1057518201
openSNPrs1057518201
23andMers1057518201
23andMe allrs1057518201
SNPshotrs1057518201
SNPdbers1057518201
MSV3drs1057518201
GWAS Ctlgrs1057518201
Max Magnitude0
ClinVar
Risk rs1057518201(-;-)
Alt rs1057518201(-;-)
Reference Rs1057518201(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131638delC
CLNSRC
CLNACC RCV000414407.1,